In recent years, the development of large-scale sequencing projects has identified numerous genomic variants in the human genome. For instance, the NyuWa genome resource (Cell Reports, 2021), led by ...
ANNOVAR® (1) provides flexibility to handle and analyze variant datasets of genomic scale. Here we make use of ANNOVAR®’s capabilities to understand a breast cancer variant dataset by applying its ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback